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PMID: 1779650 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Familial combined hyperlipidaemia: use of stable isotopes to demonstrate overproduction of very low-density lipoprotein apolipoprotein B by the liver.

Journal of inherited metabolic disease ·Vol. 14 ·No. 6 ·1991-00-00 ·Pages 915-22

Cortner JA, Coates PM, Bennett MJ, Cryer DR, Le NA

Abstract

We have assessed very low-density lipoprotein apolipoprotein B production, using [15N]glycine as an endogenous marker in a 9-hour primed constant infusion protocol, in four adult male subjects with familial combined hyperlipidaemia and in four normolipidaemic adult male controls. The mean very low-density lipoprotein apolipoprotein B absolute synthetic rate was significantly greater in the familial combined hyperlipidaemic subjects than in control subjects (26.31 +/- 8.37 vs 9.36 +/- 4.07 mg/kg per 24 h, p less than 0.05). These results confirm findings using exogenous radioisotope labelling techniques that very low-density lipoprotein apolipoprotein B production is significantly increased in most patients with familial combined hyperlipidaemia. A modified 9-hour protocol can be safely done repeatedly and in children and pregnant women.

MeSH Terms
Adult Apolipoproteins B/biosynthesis Cholesterol/blood Glycine/metabolism Humans Hyperlipidemia, Familial Combined/metabolism Lipoproteins, VLDL/biosynthesis Liver/metabolism Male Nitrogen Isotopes Triglycerides/blood
Chemicals
Apolipoproteins B Lipoproteins, VLDL Nitrogen Isotopes Triglycerides Cholesterol Glycine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Cortner J A
Lipid-Heart Research Center, Children's Hospital of Philadelphia, PA 19104.
Coates P M
Bennett M J
Cryer D R
Le N A
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Article Info
Journal
Journal of inherited metabolic disease
Abbr.
J Inherit Metab Dis
ISSN
0141-8955
Published
1991-00-00
Pages
915-22
Language
English
Region
United States
NLM ID
7910918
Subset
IM
Grants
NHLBI NIH HHS · HL-37435 · United States
NCRR NIH HHS · RR-00240 · United States
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